A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14107468



Internal ID21290717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:36891824..36902808hg38UCSC Ensembl
Innerchr4:36893446..36904430hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3810985
hg1910985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3117503
Supporting Variants
Samplessample63
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)nssv14107468
Frequency
Sample Size467
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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